Disease #03937 (IHPRF1 (hypotonia, infantile, with psychomotor retardation and characteristic facies, type 1 (IHPRF-1)), OMIM:615419)

Official abbreviation IHPRF1
Name hypotonia, infantile, with psychomotor retardation and characteristic facies, type 1 (IHPRF-1)
OMIM ID 615419
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 4
Associated with 1 gene NALCN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00080952 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - IHPRF1 Hypotonia, infantile, with psychomotor retardation and characteristic facies (OMIM:615419) NALCN NALCN 1 1 Daniel Trujillano
00380803 ? PubMed: Nair 2018 - ? - Lebanon - - - - - IHPRF1 DD; ID; hypotonia, regression; dysmorphic facial features (Neurological) - NALCN 1 1 LOVD
00391857 228P - - F no Spain - - - - - CLIFAHDD, IHPRF1 - - NALCN, PC 3 1 Alejandro Brea-Fernández
00408029 IHPRF1_F1 - Family with affected male child M ? Egypt - - - - - IHPRF1 - NALCN NALCN 1 2 Alaaeldin Fayez
00433661 - - - - - - - - - - - IHPRF1 severe intellectual disability, developmental delay - NALCN 2 1 Marketa Wayhelova
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